US3271334A - Process for the production of crosslinked compound polymers of polyacrolein - Google Patents

Process for the production of crosslinked compound polymers of polyacrolein Download PDF

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Publication number
US3271334A
US3271334A US306611A US30661163A US3271334A US 3271334 A US3271334 A US 3271334A US 306611 A US306611 A US 306611A US 30661163 A US30661163 A US 30661163A US 3271334 A US3271334 A US 3271334A
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compound
polyacrolein
polymers
produced
solution
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Kern Werner
Schulz Rolf
Loflund Irmela
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Evonik Operations GmbH
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Degussa GmbH
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2/00—Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
    • C08G2/06—Catalysts
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2/00—Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
    • C08G2/14—Polymerisation of single aldehydes not provided for in groups C08G2/08 - C08G2/12
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G81/00—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
    • C08G81/02—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers at least one of the polymers being obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D129/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Coating compositions based on hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Coating compositions based on derivatives of such polymers
    • C09D129/12—Homopolymers or copolymers of unsaturated ketones

Definitions

  • the present invention relates to a novel process for the production of cross-linked compound polymers of polyacrolein.
  • grafted polymerizates have been known to the art for some time. These grafted polymers are so constructed that the macromole-cule consists, in part, of relatively long, side chains built up from one or more foundation units which are different from the foundation units of the principal chain. Polymers of this type distinguish themselves notably from other polymers by virtue of their special, significant technical properties. Various procedures have been devised for the production of these grafted polymers.
  • the present invention relates to a novel process for the production of a variation of a type of these grafted polymers, that is, cross-linked compound polymers.
  • the cross-linked compound polymers contemplated according to the invention are in general somewhat similar to the above mentioned grafted polymers. However, there is a basic distinction between them in that the cross-linked compound polymers produced by the novel process of this invention are composed of macromolecular components which are linked with one another by very many, usually at least more than four, linkages or cross-linkages. In this way an intimately interwoven molecular structure is attained.
  • the cross-linkage are created by chemical reactions. Both components must be polymeric materials each macromolecule of which possesses more than four reactive groups.
  • the invention relates therefore to the reaction between two or more macromolecular materials which contain reactive groups.
  • the cross-linked compound polymers according to the invention are produced by the reaction of macromolecular homopoly-merization productions of acrolein (hereafter called Compound A) with at least one other polymer (hereafter called Compound B) which must contain, per macromolecule, more than four reactive groups which are able to react with aldehyde groups.
  • Compound A polymers are all macromolecular homopolymerization products of acrolein which contain, along a p-araflin type principal chain, a large number of reactive carbonyl groups, which may also be in a masked form, and are produced with free radical polymerization catalysts, preferably of the redox type.
  • Such homopoly- BZHJM Patented Sept. 6, 1966 mers are in'fusible and insoluble in organic solvents. According to the invention, however, they are employed as aqueous solutions in the form of their adducts with sulfurous acid.
  • the macromolecular homopolymers of acrolein concerned according to the invention have molecular weights of the order of 10,000 and higher (see Staudinger in Zeit. f. Angew. Chemie 49, page 802, 1936, and Staudinger, Makromolekulare Chemie & Biologie, page 6, 1947, Basel).
  • the polymeric materials (Compound B) which are reacted with the homopolymerization products of acrolein (Compound A) as contemplated according to the invention include all natural or synthetic polymers which contain groups which will react with carbonyl groups. These carbonyl reactive groups include, in particular, OI-I, SH, NH NH, NH NH groups or activated OH groups. Various combinations of these groups can be simultaneously present in one such polymer (Compound B).
  • Compound B materials within the scope of this invention are cellulose, starch, 'alginic acid, pectin, polyvinyl alcohol, polyethylene imine, collagen, gelatine, albumin, globulin, wool, especially that type of woolen goods which are known by the tradename or trademark Moreno, which are produced, as is commonly known, using animal hides as the starting material, lignin, natural or synthetic casein, particularly also keretin, proteins and the like.
  • inorganic polymers such as polymeric silicic acid, for example in the form of a silica gel or the trademarked goods Aerosil, and the like, can also be used as a Compound B polymer within the scope of this invention.
  • the process of this invention can be so conducted, that in addition to Compound A polyacrolein being in solution, the Compound B polymers can be used in a dissolved form.
  • the solvent or solvents used for this purpose must be such as will not inactivate the reactive groups of both Compounds A and B.
  • the polyacrolein solution employed according to the invention can, for example, be formed in the following manner. At the termination of the polymerization reaction by which the Compound A polyacrolein is formed and which, if desired, is conducted in the presence of water and emulsifiers, sufficient quantities of sulfur dioxide, in gaseous form, are introduced into the polyacrolein reaction mixture and the mixture is stirred at room temperature until the Compound A polyacrolein dissolves in the aqueous sulfurous acid. It is also possible, instead of S0 in gaseous form, to introduce an aqueous solution of alkali bisulfite into the polyacrolein mixture and to acidify this solution to a p of l to 5. The entire mixture can then be reacted with the Compound B polymers.
  • polyacrolein polymers react with sodium 'bisulfite to give water soluble addition compounds from which the aldehydes may be regenerated with either acid or alkali (US. Patent 2,657,192).
  • the acidified bisulfite mixture with the regenerated polyacrolein is not able to react with other macromolecular materials.
  • the proportional quantities, of each of the two reactant Compounds A and B to be used can be varied in each case over wide ranges of concentrations depending on the intended use that is to be made of the final product. It is sufiicient to add even less than 1% polyacrolein as Compound A in order to obtain measurable changes in the properties of the other Compound B polymer components.
  • the quantities in which the Compounds A and B are used are not limited, they are preferably used in a ratio of from about 1:3 to about 1:50, in case the components A and B are both used in the dissolved state.
  • a particular advantage of the cross-linked compound polymers produced according to the invention is that they can still contain a large number of reactive aldehyde groups. These reactive aldehyde groups can subsequently be subjected to further chemical reactions with such compounds as will react with aldehyde groups, as, for example, were described in German Patent 1,016,020.
  • the presence of the aldehyde groups in the cross-linked compound polymers produced according to the invention can be qualitatively proven with known carbonyl detecting reagents, for example, these compound polymers become colored to a more or less intense blue color when treated with fuchsin-sulfurous acid depending on their aldehyde group content.
  • the aldehyde groups are converted into hydroxamic acid groups, which when treated with iron III chloride solutions yield red brown colored polymeric complex salts.
  • cross-linked compound polymers can be used as hair grooming agents or as additional components in known hair treating agents.
  • the new cross-linked compound polymers produced according to the invention display properties which are not evident in either or both of the component compounds, A and B.
  • EXAMPLE 1 (a) Production of a polyacroleill-sulfurous acid solution (Compound A) according to the inventi0n.Gaseous sulfur dioxide was introduced into distilled water at 20 C. until an 8% solution of sulfurous acid was formed. 10 parts of this 8% sulfurous acid solution were added to 1 part polyacrolein which was produced by a redox polymerization of acrolein in an aqueous medium with the aid of a redox system composed of potassium persulfate and silver nitrate. The mixture was allowed to stand at room temperature. It immediately formed a viscous jelly mass which turned into a viscous solution in the course of 24 hours. Small amounts of undissolved components were then separated.
  • EXAMPLE 2 25 parts of an aqueous 15% polyvinyl alcohol solution (Compound B) were mixed at room temperature with 8 parts of a 10% polyacrolein-sulfurous acid solution (Compound A) produced as in Example 1. The mixture was stirred well and using Well known techniques was poured out to form a film. The poured solution congealed to a jelly and after being dried the film was stretchable. This film was insoluble in boiling water, acids and caustic. The presence of aldehyde groups were ascertained both by the color reaction with fuchsin-sulfurous acid as well as by the Angeli-Rimini reaction.
  • the stretchability and tensile strength of this film depends on the mol weights of polyvinyl alcohol and polyacrolein employed in the mixture of the two compounds. As the polyacrolein content increases the stretchability of the final film product decreases and the tensile strength increases. With a 30% acrolein content the tensile strength of the film produced was about three times as great as when a 1% polyacrolein content was used.
  • EXAMPLE 3 A 10% solution of gelatine (Compound B) was poured out onto glass plates and allowed to dry at room temperature.
  • the gelatine filmed glass plates were put in a Water bath at room temperature for /2 hour and were then placed in a mixture of 5 parts of a 10% polyacroleinsulfurous acid solution (Compound A) (as produced in Example 1) and 5 parts of water for /2 hour at room temperature.
  • the film was washed off and dried at room temperature. Tests with fuchsin-sulfurous acid reagent indicated that the polyacrolein had only reacted with the gelatine on the surface of the film coating.
  • the gelatine film thus produced was insoluble in water.
  • EXAMPLE 4 Cellulose (Compound B) was mercerized with 20% sodium hydroxide for 15 minutes at room temperature. It was then washed with water and dilute acetic acid after Which it was mixed with a 10% polyacrolein-sulfurous acid solution (Compound A) (produced as in Example 1). This mixture was held at room temperature for 24 hours. After this reaction period the mixture was washed with water until the wash water was free of sulfur dioxide. Aldehyde groups were thereby fixed on the cellulose thus treated and the presence of these groups was ascertainable by the customary tests, such as the use of fuchsin-sulfurous acid reagent.
  • the mercerization can also be conducted using Weaker caustic solutions and correspondingly longer reaction times.
  • EXAMPLE 5 A film of natural protein composed of beef ten-don collagen (Compound B) was first washed with water and then shaken for 20 hours at room temperature with a mixture of 20 par-ts of a 10% polyacrolein-sulfurous acid solution (Compound A) (produced as in Example 1) and 20 parts of water. After the film was washed with water to free it of sulfur dioxide its fixed aldehyde group content was qualitatively detected using the fuchsin-sulfurous acid reagent. The shinking temperature of the treated film was 7275 C. The untreated film had a shrinking temperature of 42-45 C.
  • Aqueous solutions of albumin or globulin (Compound B) when mixed with polyacrolein-sufurous acid solutions (Compound A) under the same test conditions as used above in this example, yielded insoluble precipitates at once. This was also the case when solutions of polyethylene imine were mixed with the polyacrolein-sulfurous acid solutions.
  • EXAMPLE 7 A 510% aqueous solution of polyacrylic acid hydrazide (Compound -B) was reacted with an about 10% polyacrolein-sulfurous acid solution (Compound A) at room temperature. A white precipitate formed at once, which was insoluble in all solvents.
  • the polyacrylic acid hydrazide was produced in the following manner. 5 g. of the finest possible comminuted polyacrylic acid ester were heated on a boiling water bath with 5 g. of hydrazine hydrate, until a homogeneous solution was obtained (about 2 /2 hours), which was then in turn poured into 500 cc. of methanol which contained 1 cc. of glacial acetic acid. The raw product was dissolved in 50 cc. of water and reprecipitated in methanol. After being removed by suction the precipitated polyacrylic acid hydrazide was washed with methanol and dried in a vacuum over sulfuric acid.
  • EXAMPLE 9 The presence of unreacted aldehyde groups was detected in the cross-linked compound polymers produced by this novel process by the color reaction induced with the use of fuchsin-sulfurous acid.
  • the cross-linked compound polymer produced in Example 5 from the beef tendon collagen and polyacroleinsulfurous acid solution was suspended in fuchsia-sulfurous acid reagent.
  • the aldehyde groups present in the crosslinked compound polymer reacted with this reagent and yielded a bright blue-violet colored material, the color of which was chemically combined with the polymer and could not be washed off.
  • EXAMPLE -10 The unreacted aldehyde groups present in the crosslinked compound polymers produced by the process of the invention can be further reached chemically. They can be converted, for example, into hydroxamic acid groups as was demonstrated by the following procedure.
  • the cross-linked compound polymer produced in Example 2 was mixed with an alcoholic solution of benzosulfo hydroxamic acid. After this about /2 cc. of 2 N sodium hydroxide was added with cooling and agitation and the mixture was allowed to stand at room temperature for '15 minutes. The unreacted aldehyde groups present in the cross-linked compound polymer were thus transformed into hydroxamic acid groups. These hydroxamic acid groups can be detected by an intense red coloration which occurs upon acidification with dilute hydrochloric acid and the addition of ferric chloride solution. 9
  • the products can be used as filter which additionally shows the properties of the polyacrolein.
  • the stretchable film which has been produced according to Example 2 can be used as transparent packing material.
  • EXAMPLE I (a) Production of an acidified polyacrolein-bisulfite solution (Compound A) according to the invention-35 cc. of water were added to 3.5 g. polyacrolein (which was produced by a redox polymerization of acrolein in an aqueous medium with the aid of a redox system com posed of potassium persulfate and silver nitrate) and 5 g. of Na S O The mixture was heated at 50 C. for 4 hours. 10 cc. of a 2 normal solution of hydrochloric acid were then added to the limpid solution. The p of the mixture was 1.
  • EXAMPLE 12 the same manner as in Example 11b. Its properties were the same as the properties of the film obtained according to Example 11b.
  • EXAMPLE 13 An albuminous substance in form of a foil produced from sinew collagen was immersed into the polyacroleinbisulfite solution corresponding to Example 12a for 10 hours at room temperature. Then the foil was washed with water for 24 hours and dried.
  • the aldehyde groups of the polyacrolein were thereby chemically bound on molecular weight of at least 10,000 produced in the presence of a free radical polymerization catalyst dissolved in an acid aqueous solution of sulfurous acid having a pH between 1 and 5 with a polymeric compound selected from the group consisting of natural and synthetic polymeric compounds which are macromolecular and contain more than four groups per macromolecule which are reactive with aldehyde groups selected from the group consisting of H, SH, NH NH, NH --NH and activated CH groups at a temperature between 0 and 200 C.
  • a process as in claim 5 further comprising removing all 80;, from said homopolymer of acrolein solution before said reaction, said homopolymer of acrolein 8 being rendered thereby into a stable reactive hydrate form.
  • a process for the production of cross-linked compound polymers which comprises reacting an infusible macromolecular homopolymer of acrolein, having a molecular weight of at least 10,000 produced in the presence of a free radical polymerization catalyst, dissolved in an acid aqueous solution of sulfurous acid having a pH be tween 1 and 5 with a polymeric compound which is macromolecular and contains more than four groups per macromolecule which are reactive With aldehyde groups selected from the group consisting of cellulose, starch, alginic acid, pectin, polyvinyl alcohol, polyethylene imine, proteins, lignin and polymeric silicic acid at a temperature between 0 and 200 C. in a proportion of about 1 part by weight of dissolved acrolein polymer per 3 to parts by weight of the polymeric compound containing the groups which are reactive with aldehyde groups.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
US306611A 1958-10-04 1963-09-04 Process for the production of crosslinked compound polymers of polyacrolein Expired - Lifetime US3271334A (en)

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DED29076A DE1083051B (de) 1958-10-04 1958-10-04 Verfahren zur Herstellung von Verbundpolymeren des Polyacroleins

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3397172A (en) * 1963-02-16 1968-08-13 Degussa Process for the preparation of polyacrolein gels and process for improving the properties and sealing of soils, soil formations, structures, structural elements and structural materials
US3770588A (en) * 1972-10-02 1973-11-06 American Cyanamid Co Storage stabilization of carrier bound enzymes
US3965070A (en) * 1974-10-07 1976-06-22 Rohm And Haas Company Crosslinked vinylcarbonyl resins having α-amino acid functionality
WO2000047149A1 (en) 1999-02-11 2000-08-17 Hydromer, Inc. Gels formed by the interaction of poly(aldehyde) with various substances
CN111467949A (zh) * 2020-03-30 2020-07-31 深圳华明环保科技有限公司 一种二噁英抑制剂及其制备方法与应用

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE624108A (is") * 1961-10-28
BE635438A (is") * 1962-07-28

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2657192A (en) * 1951-01-25 1953-10-27 Du Pont Polymerization of acrolein
DE1082408B (de) * 1956-04-12 1960-05-25 American Cyanamid Co Polymerisierungsverfahren
US3030319A (en) * 1958-10-13 1962-04-17 American Cyanamid Co Process for polymerization of a vinylidene monomer in the presence of a cobaltic salt and an organic reducing agent

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1064715B (de) 1957-10-05 1959-09-03 Hoechst Ag Verfahren zur Herstellung von wasserbestaendigen, geformten Gebilden

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2657192A (en) * 1951-01-25 1953-10-27 Du Pont Polymerization of acrolein
DE1082408B (de) * 1956-04-12 1960-05-25 American Cyanamid Co Polymerisierungsverfahren
US3030319A (en) * 1958-10-13 1962-04-17 American Cyanamid Co Process for polymerization of a vinylidene monomer in the presence of a cobaltic salt and an organic reducing agent

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3397172A (en) * 1963-02-16 1968-08-13 Degussa Process for the preparation of polyacrolein gels and process for improving the properties and sealing of soils, soil formations, structures, structural elements and structural materials
US3770588A (en) * 1972-10-02 1973-11-06 American Cyanamid Co Storage stabilization of carrier bound enzymes
US3965070A (en) * 1974-10-07 1976-06-22 Rohm And Haas Company Crosslinked vinylcarbonyl resins having α-amino acid functionality
WO2000047149A1 (en) 1999-02-11 2000-08-17 Hydromer, Inc. Gels formed by the interaction of poly(aldehyde) with various substances
EP1164991A4 (en) * 1999-02-11 2006-07-19 Hydromer Inc GELS MADE BY THE INTERACTION OF POLYALDEHYDE WITH DIFFERENT SUBSTANCES
CN111467949A (zh) * 2020-03-30 2020-07-31 深圳华明环保科技有限公司 一种二噁英抑制剂及其制备方法与应用

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DE1083051B (de) 1960-06-09
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NL243578A (is")

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